International Patient Summary Implementation Guide (Release 0.3.0 STU1 Ballot)

International Patient Summary Implementation Guide, published by Health Level Seven International - Patient Care Work Group. This is not an authorized publication; it is the continuous build for version 0.3.0). This version is based on the current content of https://github.com/HL7/fhir-ips/ and changes regularly. See the Directory of published versions

International Patient Summary Implementation Guide

An International Patient Summary (IPS) document is an electronic health record extract containing essential healthcare information about a subject of care. As specified in EN 17269 and ISO/CD 27269, it is designed for supporting the use case scenario for ‘unplanned, cross border care’, but it is not limited to it. It is intended to be international, i.e., to provide generic solutions for global application beyond a particular region or country.

The IPS dataset is minimal and non-exhaustive; specialty-agnostic and condition-independent; but still clinically relevant.

The IPS document is composed by a set of robust, well-defined and potentially reusable core sets of data items (indicated as IPS library in the figure below). The tight focus of the IPS on unplanned care is in this case not a limitation, but, on the contrary, facilitates their potential re-use beyond the IPS scope.

Figure 1: The IPS product and by-products
IPS_doc_library.png

Purpose

The goal of this Implementation Guide is to specify how to represent in HL7 FHIR the International Patient Summary (IPS). An alternative representation as templated HL7 CDA R2 is also provided ( see the hl7.org site or ART DECOR. The initial focus of the International Patient Summary (IPS) was the unplanned care across national borders. Starting from this focus, the specification is intended to be used and be useful in local applications and also to be supportive of planned care.

Project Background

See further details on the project background in the IPS Wiki here.

Project Scope

As specified in the CEN EN 17269 and ISO/CD 27269, the IPS dataset is a “minimal, non-exhaustive set of data elements required for the international patient summary”.

‘Minimal’ reflects the ideas of ‘summary’ and the need to be concise, but also alludes to the existence of a core set of data elements that all health care professionals can use; it is intended to be a speciality agnostic and condition independent set. It does not imply that all the items in the data set will be used in every summary. It is also possible to refine the extract from a record such that the content of the summary is more relevant to a particular condition (e.g. asthma) but no asthma-specific elements will be specified in this standard. The IPS Document or IPS can be extended by non-IPS standard condition-specific data. ‘Non-exhaustive’ recognizes that the ideal data set is not closed, and is likely to be extended, not just in terms of requirement evolution, but also pragmatically in instances of use. [EN 17269; ISO/CD 27269].

Furthermore the scope of the IPS is global. Although this is a major challenge, this implementation guide takes various experiences and newer developments (e.g. US Core Implementation Guide (FHIR IG)) into account to address global feasibility as far as possible.

The following picture provides an overview of the current IPS content.

Figure 2: The IPS composition
IPS_composition.png

Relationships with Other Projects and Guidelines

See further details on the IPS project relationships with other projects and guidelines in the IPS Wiki here.

Ballot Status

This Implementation Guide is being balloted as STU with the intention to go normative in a subsequent ballot cycle.

Authors and Contributors

Role Name Organization contact
Primary Editor Giorgio Cangioli, PhD Consultant, HL7 Italy giorgio.cangioli@gmail.com
Primary Editor Rob Hausam Hausam Consulting LLC rob@hausamconsulting.com
Primary Editor François Macary Phast francois.macary@phast.fr
Contributor Dr Christof Geßner Gematik christof.gessner@gematik.de
Contributor Gary Dickinson CentriHealth gary.dickinson@ehr-standards.com
Contributor Dr Kai U. Heitmann Heitmann Consulting and Services, Gefyra GmbH, HL7 Germany info@kheitmann.de
Contributor Catherine Chronaki HL7 International Foundation chronaki@gmail.com
Contributor George Dixon Allscripts LLC george.dixon@allscripts.com
Contributor Kenneth Sinn eHealth Ontario ken.sinn@ehealthontario.on.ca